Perspectives on push–pull chromophores derived from click-type [2 + 2] cycloaddition–retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes

Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and notew...

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Published inBeilstein journal of organic chemistry Vol. 20; no. 1; pp. 125 - 154
Main Author Yamada, Michio
Format Journal Article
LanguageEnglish
Published Germany Beilstein-Institut 22.01.2024
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Online AccessGet full text
ISSN1860-5397
1860-5397
DOI10.3762/bjoc.20.13

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Abstract Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and noteworthy advancements in the research on push–pull chromophores prepared via the [2 + 2] CA–RE reaction is conducted. In particular, an overview of the physicochemical properties of the family of these compounds that have been investigated is provided to clarify their potential for future applications.
AbstractList Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions involving diverse electron-rich alkynes and electron-deficient alkenes. In this review, a comprehensive investigation of the recent and noteworthy advancements in the research on push–pull chromophores prepared via the [2 + 2] CA–RE reaction is conducted. In particular, an overview of the physicochemical properties of the family of these compounds that have been investigated is provided to clarify their potential for future applications.
Author Yamada, Michio
AuthorAffiliation 1 Department of Chemistry, Tokyo Gakugei University, Nukuikitamachi 4-1-1, Koganei, Tokyo 184-8501, Japan https://ror.org/00khh5r84 https://www.isni.org/isni/0000000107205963
AuthorAffiliation_xml – name: 1 Department of Chemistry, Tokyo Gakugei University, Nukuikitamachi 4-1-1, Koganei, Tokyo 184-8501, Japan https://ror.org/00khh5r84 https://www.isni.org/isni/0000000107205963
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/38292046$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords click chemistry
photoinduced electron transfer
donor–acceptor conjugate
photoluminescence
intramolecular charge transfer
Language English
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Snippet Various push–pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition–retroelectrocyclization (CA–RE) reactions...
Various push-pull chromophores can be synthesized in a single and atom-economical step through [2 + 2] cycloaddition-retroelectrocyclization (CA-RE) reactions...
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StartPage 125
SubjectTerms Chemistry
click chemistry
donor–acceptor conjugate
intramolecular charge transfer
photoinduced electron transfer
photoluminescence
Review
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Title Perspectives on push–pull chromophores derived from click-type [2 + 2] cycloaddition–retroelectrocyclization reactions of electron-rich alkynes and electron-deficient alkenes
URI https://www.ncbi.nlm.nih.gov/pubmed/38292046
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